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2023 | 3 |
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Page 1
A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX: a case report and literature review.
Blood Press. 2023 Dec;32(1):2195008. doi: 10.1080/08037051.2023.2195008.
Blood Press. 2023.
PMID: 37088984
Review.
Glp-1 Receptor Agonists Regulate the Progression of Diabetes Mellitus Complicated with Fatty Liver by Down-regulating the Expression of Genes Related to Lipid Metabolism.
Zheng S, Huang H, Chen H, Liu Y.
Zheng S, et al. Among authors: chen h.
Appl Biochem Biotechnol. 2023 Aug;195(8):5238-5251. doi: 10.1007/s12010-023-04505-x. Epub 2023 May 4.
Appl Biochem Biotechnol. 2023.
PMID: 37140780
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Circ_0104652 promotes the proliferation and migration of ox-LDL-stimulated vascular smooth muscle cells via stabilizing ADAMTS7 and HMGB1.
Bian B, Chen H, Teng T, Huang J, Yu X.
Bian B, et al. Among authors: chen h.
Am J Hypertens. 2024 Mar 27:hpae026. doi: 10.1093/ajh/hpae026. Online ahead of print.
Am J Hypertens. 2024.
PMID: 38536049
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Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report.
Chen H, Yao W, He Q, Yu X, Bian B.
Chen H, et al.
BMC Med Genet. 2020 May 27;21(1):116. doi: 10.1186/s12881-020-01049-3.
BMC Med Genet. 2020.
PMID: 32460727
Free PMC article.
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New Insights into Radio-Resistance Mechanism Revealed by (Phospho)Proteome Analysis of Deinococcus Radiodurans after Heavy Ion Irradiation.
Liu S, Wang F, Chen H, Yang Z, Ning Y, Chang C, Yang D.
Liu S, et al. Among authors: chen h.
Int J Mol Sci. 2023 Oct 1;24(19):14817. doi: 10.3390/ijms241914817.
Int J Mol Sci. 2023.
PMID: 37834265
Free PMC article.
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